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NEXTSEQ™ 1000/2000 INDEX PRIMER KIT - INVIMA Registration e4fbba4cb9969e5fa536853efb081165

Access comprehensive regulatory information for NEXTSEQ™ 1000/2000 INDEX PRIMER KIT (NEXTSEQ™ 1000/2000 INDEX PRIMER KIT ) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID e4fbba4cb9969e5fa536853efb081165 and manufactured by ILLUMINA COLOMBIA S.A.S.. The device was registered on February 14, 2033.

This page provides complete registration details including product type (REACTIVOS IN VITRO), authorised information, and regulatory compliance data from the official Colombia INVIMA medical device database. Pure Global AI offers free access to Colombia's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate INVIMA regulations efficiently.

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INVIMA Official Data
I
e4fbba4cb9969e5fa536853efb081165
NEXTSEQ™ 1000/2000 INDEX PRIMER KIT
INVIMA Analysis ID: e4fbba4cb9969e5fa536853efb081165
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Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
REACTIVOS IN VITRO
Product Type (English)
REACTIVOS IN VITRO
Registration Information
Analysis ID
e4fbba4cb9969e5fa536853efb081165
Expire Date
February 14, 2033
Authorized Company / Fabricante
Name (English)
ILLUMINA COLOMBIA S.A.S.